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NDT Plus 2008 1(Supplement 3):iii54-iii58; doi:10.1093/ndtplus/sfn088
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© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

This article appears in the following NDT Plus issue: Parathyroid Intervention - Current themes and future perspectives [View the issue table of contents]

Reversed whole PTH/intact PTH ratio as an indicator of marked parathyroid enlargement: five case studies and a literature review

Hirotaka Komaba1, Yoko Takeda1, Jeongsoo Shin2, Reika Tanaka3, Takatoshi Kakuta3, Yoshihiro Tominaga4 and Masafumi Fukagawa1

1 Division of Nephrology and Kidney Center, Kobe University School of Medicine, Kobe 650-0017
2 Motomachi HD Clinic, Kobe, 650-0012
3 Department of Internal Medicine, Tokai University School of Medicine, Isehara, 259-1193
4 Department of Transplant and Endocrine Surgery, Nagoya Second Red Cross Hospital, Nagoya, 466-8650, Japan

Correspondence: Masafumi Fukagawa, Division of Nephrology and Kidney Center, Kobe University School of Medicine, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan. Tel: +81-78-382-6500; Fax: +81-78-382-6509; E-mail: fukagawa{at}med.kobe-u.ac.jp


   Abstract
Top
 Abstract
Introduction
 Case reports
 Discussion
 References
 
Parathyroid hormone (PTH) levels detected by intact PTH assays are generally higher than those detected by the whole PTH assay because the latter does not detect non-(1–84) PTH fragments, mainly PTH (7–84). Rare exceptions to this rule have been reported in patients with severe primary or secondary hyperparathyroidism and parathyroid carcinoma. Overproduction of an N-form of PTH other than PTH (1–84) has been observed in the sera of these patients. We report five additional cases with the reversed whole PTH/intact PTH ratio associated with severe hyperparathyroidism in haemodialysis patients. Three patients demonstrated enlargement of a single hypervascular gland, whereas the other two had undergone surgical parathyroidectomy and later showed recurrent hyperparathyroidism due to progressive autograft hyperplasia. In the case of a single enlarged gland, the pathological pattern and heterogeneous expression of parathyroid adenomatosis 1/cyclin D1 suggested it to be a single nodule of uraemic hyperparathyroidism rather than sporadic primary adenoma. These cases suggested that the reversed whole PTH/intact PTH ratio could be an indicator of marked parathyroid enlargement. Further studies are required to elucidate the clinical significance of the reversed whole PTH/intact PTH ratio in haemodialysis patients.

Key Words: intact PTH • N-PTH • secondary hyperparathyroidism • single nodule • whole PTH

Received for publication February 5, 2008. Accepted for publication February 29, 2008.


   Introduction
Top
 Abstract
 Introduction
Case reports
 Discussion
 References
 
Disorder of mineral and bone metabolism is one of the most prevalent and serious abnormalities in dialysis patients. Second-generation parathyroid hormone (PTH) assays, also called intact PTH assays, have been widely used for optimal management of parathyroid function and bone remodelling [1–3]. Until recently, these assays were believed to react only with full-length PTH (1–84); however, they also detect large C-terminal fragments with a partially preserved N-terminal structure, mainly PTH (7–84) [4,5]. This is especially relevant in dialysis patients because reduced clearance from the kidneys may result in increased levels of these fragments [6]. Moreover, PTH (7–84) has been shown to antagonize the calcaemic and bone-resorbing effects of PTH (1–84) [7, 8].

Third-generation PTH assays, such as the whole PTH assay or bio-intact PTH assay, have recently been developed to overcome such complex methodological and biological problems. These assays are more sensitive and specific when measuring bioactive PTH (1–84) [9,10]. PTH values obtained from intact PTH assays are generally higher than those obtained from the whole PTH assay because the latter does not detect non-(1–84) fragments [10–13]. Rare exceptions to this rule have been reported in patients with severe primary and secondary hyperparathyroidism and parathyroid cancer [14–19]. Moreover, a new molecular form of N-PTH, distinct from PTH (1–84), has been identified in the circulation after HPLC fractionation of serum [14–16,18].

We present a series of cases with progressive hyperparathyroidism in whom whole PTH levels were paradoxically higher than intact PTH levels. We then reviewed the recent literature and summarized the clinical features of published cases with the reversed whole PTH/intact PTH ratio, which suggested that this reversed ratio could be a marker for the severity of hyperparathyroidism.


   Case reports
Top
 Abstract
 Introduction
 Case reports
Discussion
 References
 
Case 1
A 55-year-old male had been receiving haemodialysis since February 2003 for end-stage renal disease (ESRD) due to diabetic nephropathy. In May 2006, on detection of high intact PTH levels (327 pg/ml; Elecsys PTH; Roche Diagnostics, Mannheim, Germany) the patient was treated with intravenous calcitriol (1.0 µg/week). However, serum intact PTH levels progressively increased to 528 pg/ml and abnormally elevated levels of whole PTH (614 pg/ml; Whole PTH; Scantibodies Laboratories, Santee, CA, USA) were found. Serum bone alkaline phosphatase levels increased to 46 U/l. Doppler ultrasonography showed a single enlarged hypervascular parathyroid gland (14 mm x 11 mm x 7 mm). Surgical parathyroidectomy was performed, and the intact and whole PTH levels decreased to 17 and 5.9 pg/ml, respectively, with normalization of the reversed whole PTH/intact PTH ratio (Figure 1).


Figure 1
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  		Fig. 1 Serum PTH levels before and after parathyroidectomy. Reversed whole PTH/intact PTH ratio normalized after surgery, as is usual in uraemic patients.

 
The resected gland showed hyperplasia of the parathyroid cells without the normal rim, supporting the diagnosis of secondary hyperparathyroidism (Figure 2A). However, the complication of sporadic primary adenoma remains a possibility in dialysis patients, especially those with a single enlarged gland. Thus, we performed immunohistochemical analysis, which is known to be helpful when differentiating these two disorders, as previously reported by Tominaga et al. [20]. The immunostaining pattern of Ki-67 indicated accelerated cell growth progression (labelling index 28/1000) (Figure 2B), while heterogeneous expression of parathyroid adenomatosis 1/cyclin D1 was not consistent with primary adenoma (labelling index 360/1000) (Figure 2C). Thus, the gland was diagnosed as a single nodule, the most advanced type of parathyroid hyperplasia in chronic uraemic patients.


Figure 2
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  		Fig. 2 (A) Histological findings of the resected parathyroid gland. Note the single nodular hyperplasia of the parathyroid cells without the normal rim. Carcinomatous changes are not evident. (B) Immunohistochemical findings of Ki-67 indicate accelerated cell growth progression (labelling index 28/1000). (C) Heterogeneous expression of parathyroid adenomatosis 1/cyclin D1 (labelling index 360/1000) suggesting a single nodule of uraemic hyperparathyroidism rather than a sporadic primary adenoma.

 
Case 2
A 58-year-old female had been receiving haemodialysis since May 1996 for ESRD due to IgA nephropathy. In February 2007, despite maintenance of intact PTH levels (178 pg/ml; Elecsys PTH) and whole PTH levels (134 pg/ml), routine Doppler ultrasonography revealed a hypervascular enlarged gland (14 mm x 12 mm x 12 mm). With the intention of preventing the progression of secondary hyperparathyroidism, oral falecalcitriol (0.15 µg/day) was started; however, after 10 months of treatment, serum intact and whole PTH levels progressively increased to 685 and 704 pg/ml, respectively, with the reversed whole PTH/intact PTH ratio. Re-examination by ultrasonography showed a progressive enlargement of the parathyroid gland (18 mm x 14 mm x 14 mm) (Figure 3A), and a hot spot was detected at the same location by 99mTc methoxyisobutyl-isonitrile scintigraphy (Figure 3B). Serum bone alkaline phosphatase levels increased up to 102 U/l, indicating extremely high bone turnover. Accordingly, the patient was scheduled for parathyroidectomy.


Figure 3
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  		Fig. 3 (A) Power Doppler ultrasonography showing a single enlarged hypervascular parathyroid gland (18 mm x 14 mm x 14 mm). (B) 99mTc methoxyisobutyl-isonitrile scintigraphy demonstrating a hot spot in the right inferior parathyroid gland.

 
Case 3
A 60-year-old male had been receiving haemodialysis since November 2001 for ESRD due to diabetic nephropathy. For several years, serum intact PTH levels were maintained between 200 and 300 pg/ml (Elecsys PTH). However, in June 2006, despite ideal control of parathyroid function, a routine neck ultrasonography examination revealed an enlarged hypervascular parathyroid gland (17 mm x 14 mm x 15 mm). Subsequently, secondary hyperparathyroidism rapidly advanced, and in December 2007, serum intact and whole PTH levels increased to 612 and 801 pg/ml, respectively, with the reversed whole PTH/intact PTH ratio. Significantly progressive enlargement of the parathyroid gland (23 mm x 21 mm x 21 mm) was shown by ultrasonography. Serum bone alkaline phosphatase levels increased to 54 U/l. Accordingly, the patient was scheduled for parathyroidectomy.

Case 4
A 54-year-old male had been receiving haemodialysis since 1974 for ESRD due to chronic glomerulonephritis. Since 1981, he was found to have extremely high carboxyl-terminal PTH (C-PTH) levels between 20 and 30 ng/ml (normal range, 0.2–1.0 ng/ml). Total parathyroidectomy with forearm autograft was performed in 1986, and the C-PTH levels effectively decreased to 0.5 ng/ml. The resected gland showed parathyroid hyperplasia. For about two decades after surgery, secondary hyperparathyroidism, which was evaluated by intact PTH assays, had been managed well; however, in November 2007, abnormally higher whole PTH levels (358 pg/ml) than intact PTH levels (278 pg/ml; total PTH; Scantibodies Laboratories) were found. Ultrasonography of the forearm showed an enlarged parathyroid tissue (17 mm x 7 mm x 3 mm). After informed consent was obtained, we performed a simplified Casanova test (total ischaemic blockade of the graft-bearing arm), as previously described [21]. Following temporary ischaemic autograftectomy, the intact and whole PTH levels significantly decreased to 127 and 117 pg/ml, respectively, with normalization of the reversed whole PTH/intact PTH ratio, suggesting that the autografted parathyroid tissue was the cause of the reversed ratio. The patient was then scheduled for surgical removal of the autografted gland.

Case 5
A 39-year-old female had been receiving haemodialysis since 1979 for ESRD due to chronic glomerulonephritis. In 1993, total parathyroidectomy with forearm autograft was performed for secondary hyperparathyroidism, which was then maintained for several years. However, in January 2007, elevated levels of intact PTH (396 pg/ml; Elecsys PTH), whole PTH (263 pg/ml) and bone alkaline phosphatase activity (63 U/l) were found. Ultrasonography of the graft-bearing arm showed an enlargement of the parathyroid tissue (17 mm x 16 mm x 5 mm). When PTH levels were measured in the sera obtained from the graft-bearing arm, extremely elevated levels of intact and whole PTH levels were found (3600 and 4490 pg/ml, respectively), with the reversed whole PTH/intact PTH ratio. Surgical removal of the autografted gland was performed under local anaesthesia. After surgery, the intact and whole PTH levels measured in the sera obtained from the graft-bearing arm decreased to 27 and 39 pg/ml, respectively, but without normalization of the reversed ratio. It was then suggested that small fragments of the parathyroid tissue (i.e. the probable cause of the reversed whole PTH/intact PTH ratio) remained in the forearm. As expected, recurrent hyperparathyroidism soon developed and further treatment was required.


   Discussion
Top
 Abstract
 Introduction
 Case reports
 Discussion
References
 
We report five exceptional cases with the reversed whole PTH/intact PTH ratio associated with progressive hyperparathyroidism, seen in relatively rapid succession in clinical practice. Three patients demonstrated an enlargement of a single hypervascular gland, and the pathological pattern and heterogeneous expression of parathyroid adenomatosis 1/cyclin D1 suggested it to be a single nodule of uraemic hyperparathyroidism in case 1. The other two patients had undergone surgical parathyroidectomy and subsequently showed recurrent hyperparathyroidism due to progressive autograft hyperplasia.

Abnormally higher whole PTH levels than intact PTH levels have been reported in a minority of patients with severe hyperparathyroidism and parathyroid cancer [14–19]. D’Amour et al. analysed serum samples from these patients by HPLC and were the first to identify a new molecular form of PTH with an intact N-terminal, distinct from (1–84) PTH [14–16]. More recently, we also revealed the overproduction of N-PTH in a haemodialysis patient with a single nodule of uraemic hyperparathyroidism [18]. This N-form of PTH is detectable by the whole PTH assay, but is less reactive in intact PTH assays [14–16,22]. Hence, the reversed whole PTH/intact PTH ratio strongly suggests the existence of N-PTH. This new molecular form is not produced during the peripheral metabolism of PTH (1–84) [23], while we have recently shown that the source of excess N-PTH is associated with the pathological parathyroid tissue [18].

To date, our group has reported three haemodialysis patients with severe hyperparathyroidism associated with the reversed whole PTH/intact PTH ratio [17–19]. The first [17] and second [18] cases showed a single nodule of uraemic hyperparathyroidism for which surgical parathyroidectomy was performed, and the reversed PTH ratio normalized after surgery. The third case showed excessive growth of parathyroid gland that outstripped vascular supply, and spontaneous remission due to autoinfarction of the parathyroid gland resulted in normalization of the reversed whole PTH/intact PTH ratio [19]. The clinical features of the present cases and previously published cases with the reversed whole PTH/intact PTH ratio are summarized in Table 1. All cases with the reversed whole PTH/intact PTH ratio showed progressive enlargement of the parathyroid gland. These findings are in accordance with previous cases of the reversed whole PTH/intact PTH ratio associated with clinically worse parathyroid disease [14–16]. Taken together, it is suggested that overproduction of N-PTH, represented by the reversed whole PTH/intact PTH ratio, could be an indicator of progressive hyperparathyroidism.


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  		Table 1 Clinical features of haemodialysis patients with the reversed whole PTH/intact PTH ratio: previous and present reports

 
Differential diagnosis between primary and secondary hyperparathyroidism is very difficult in dialysis patients with a single enlarged gland [20], especially those receiving haemodialysis for a long time. In this study, we performed immunohistochemical analysis to differentiate these two disorders. Consequently, the advanced type of uraemic hyperparathyroidism was corroborated by the heterogeneous expression of parathyroid adenomatosis 1/cyclin D1, one of the genetic abnormalities responsible for tumorigenesis in primary adenoma (case 1). Thus, the reversed whole PTH/intact PTH ratio is also a distinct possibility in severe type of secondary hyperparathyroidism. Surgical parathyroidectomy may be required for such patients with the reversed whole PTH/intact PTH ratio and enlarged parathyroid gland.

The physiological role of N-PTH is controversial. Recent clinical data suggest that this new form of PTH has a significant biological effect on bone turnover [18,19]. The present cases also showed relatively high serum levels of bone alkaline phosphatase compared with intact PTH levels. In clinical practice, we should remember that intact PTH assays usually overestimate the real activity of PTH on bone, as previously shown [24], but they also occasionally underestimate its activity, as the present cases. With regard to its structure, this molecular form reacts poorly in intact PTH assays, having early 12–18 or 12–24 epitopes, but normally in the Roche Elecsys assay with a 26–32 epitope, suggesting a modification in the region 15–20 [14–16,22]. The only post-translational modification ever described is phosphorylation in the N-terminal region [25]. Thus, several investigators postulated that N-PTH could be phosphorylated on Ser17 [14,16]. In our patients, however, the values of the whole PTH assay were abnormally higher than those of the Elecsys assay with a 26–32 epitope. The precise reason for this finding is unknown, but one possible explanation is diversity in the mode of modification of this molecule.

In conclusion, we report a series of five exceptional cases with the reversed whole PTH/intact PTH ratio. All cases demonstrated progressive enlargement of the parathyroid gland. It is speculated that the enlarged parathyroid gland overproduced and secreted a novel form of N-PTH. These cases suggested that the reversed whole PTH/intact PTH ratio or the overproduction of N-PTH is associated with progressive hyperparathyroidism. Moreover, the abnormally elevated whole PTH/intact PTH ratio, even if it is not reversed, might indicate progressive hyperparathyroidism [26]. Further studies are required to elucidate the clinical significance of the reversed whole PTH/intact PTH ratio in haemodialysis patients.


   Acknowledgements
 
The authors acknowledge Dr Toyonori Tsuzuki (Department of Pathology, Nagoya Second Red Cross Hospital, Nagoya, Japan) for performing immunohistochemical analysis and Mr Yasushi Shimizu (Motomachi HD Clinic, Kobe, Japan) for his expert technical assistance.

Conflict of interest statement. None declared.


   References
Top
 Abstract
 Introduction
 Case reports
 Discussion
 References
 

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